Chemical Class Description: The class of GRASP55 inhibitors comprises a diverse range of compounds that indirectly modulate the activity of GRASP55 by targeting various cellular processes and signaling pathways associated with Golgi apparatus function and vesicular trafficking. These compounds do not directly interact with GRASP55 but influence the cellular environment and mechanisms crucial for its function. Brefeldin A, Golgicide A, and Monensin disrupt the structure and function of the Golgi apparatus, thereby potentially affecting the role of GRASP55 in Golgi maintenance and assembly. Nocodazole and Vinblastine, by affecting microtubule dynamics, impact the processes of vesicular trafficking in which GRASP55 is involved.
Tunicamycin and Thapsigargin, targeting protein glycosylation and inducing ER stress respectively, can influence the protein processing and ER-Golgi interactions, thereby affecting GRASP55's activity. PI3K inhibitors like Wortmannin and LY294002, as well as the mTOR inhibitor Rapamycin, modulate signaling pathways that might influence GRASP55 function in Golgi organization and vesicle transport. Dynasore, by inhibiting Dynamin, impacts vesicle trafficking, a key process in GRASP55's function. Cytochalasin D, targeting actin polymerization, affects the cytoskeletal dynamics crucial for vesicular trafficking and thus GRASP55's role
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